- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT01342471
Physical Activity and Leisure-time Study (PALS) (PALS)
10 de octubre de 2012 actualizado por: University of Tennessee
TV Commercial Stepping: Can America's Top Sedentary Activity be Made More Active
Physical inactivity is a major public health problem and a primary contributing factor to the obesity epidemic.
While most Americans do not meet the physical activity (PA) guidelines (30 min/day, 5 day/wk), they do report watching several hours of TV each day, and frequently site "lack of time" as a barrier for engaging in PA.
The Physical Activity and Leisure-time Study examines an approach convert sedentary TV watching into active TV watching time by having adults step in place during commercials (TV commercial stepping).
Descripción general del estudio
Estado
Terminado
Condiciones
Intervención / Tratamiento
Descripción detallada
This randomized controlled trial will examine the effects of a PA prescription of TV commercial stepping for at least 90 min/day of TV programming, with that of walking at least 30 min/day (30 min walk) on daily step counts, TV viewing, and diet during a 24 week PA intervention.
Sedentary, overweight or obese, adults will be randomly assigned to either the TV commercial stepping, or 30 min walk group during a 24-week behavioral PA intervention.
Both groups will attend 8 sessions, but receive different PA goals.
PA, TV watching time, diet, and anthropometric data will be collected at 0, 12, and 24 weeks.
It is hypothesized that the TV commercial stepping condition will, show an equal increase in PA at 12 and 24 weeks as compared to the 30-min walk condition.
Neither group is hypothesized to demonstrate changes in TV viewing time, dietary intake, or weight.
Tipo de estudio
Intervencionista
Inscripción (Actual)
58
Fase
- Fase 1
Contactos y Ubicaciones
Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.
Ubicaciones de estudio
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Tennessee
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Knoxville, Tennessee, Estados Unidos, 37920
- HPER Building, 1914 Andy Holt Ave.
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Criterios de participación
Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.
Criterio de elegibilidad
Edades elegibles para estudiar
25 años a 65 años (Adulto, Adulto Mayor)
Acepta Voluntarios Saludables
No
Géneros elegibles para el estudio
Todos
Descripción
Inclusion Criteria:
- 25 to 65 years of age
- BMI between 25 and 45 kg/m2
- watch ≥14 hours per week of TV
- ability to follow instructions and record data
- ability to walk 1/4 mile without stopping
Exclusion Criteria:
- history of myocardial infraction, angina, stroke, heart failure, or uncontrolled cardiac arrhythmias
- a resting blood pressure greater than 180 mm Hg systolic and/or 100 mm Hg diastolic
- other physical or medical limitations for engaging in physical activity
- no television in the home
- baseline physical activity level exceeding 7,499 steps per day as determined by the Omron pedometer
- currently participating in a program to increase PA
- intended to move outside the East Tennessee area within the time frame of the intervention
- were pregnant, lactating, less than 6 months post-partum, or planned to become pregnant during the time frame of the intervention
- unwilling to attend group intervention meetings, assessments or to complete an activity diary for the duration of the study.
Plan de estudios
Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Tratamiento
- Asignación: Aleatorizado
- Modelo Intervencionista: Asignación paralela
- Enmascaramiento: Único
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
|---|---|
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Comparador activo: 30-min walk
Instructed to use "brisk" walking (at least 30 min/day in bouts of at least 10 min) at least 5 days/week.
Participants were permitted to exercise in one long bout (30 min) or divide the exercise into multiple bouts as long as the bout length was 10 min or greater.
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Participants were instructed to use "brisk" walking (at least 30 min/day in bouts of at least 10 min) at least 5 days/week.
Both conditions will receive an ankle mounted Omron pedometer, so they were able to track their steps each day.
Participants were not given instructions concerning diet modification or modifying TV viewing time during a 6 month behavioral physical activity intervention
Otros nombres:
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Experimental: TV commercial stepping
Instructed to stand and "briskly" step in place, or "briskly" walk continuously around the room/house for the duration of each commercial break during at least 90 min of TV programming on at least 5 days/week.
Rather than exercising continuously for at least 10-minute bouts, participants performed multiple (~9 or 10), short (~3-5 min) bouts, conveniently incorporated into their daily TV viewing time.
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Participants were instructed to stand and "briskly" step in place, or "briskly" walk continuously around the room/house for the duration of each commercial break during at least 90 min of TV programming on at least 5 days/week.
Both conditions will receive an ankle mounted Omron pedometer, so they were able to track their steps each day.
Participants were not given instructions concerning diet modification or modifying TV viewing time during a 6 month behavioral physical activity intervention
Otros nombres:
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¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Physical Activity (Steps/Day)
Periodo de tiempo: 0 and 6 months
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Change in pedometer measured steps per day between 0 and 6 months
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0 and 6 months
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Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Total Energy Intake
Periodo de tiempo: 0 and 6 months
|
Change in total energy intake(kcals/day) between 0 and 6 months
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0 and 6 months
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TV Related Energy Intake
Periodo de tiempo: 0 and 6 months
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Change in energy intake (kcals/day) while watching TV between 0 and 6 months
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0 and 6 months
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Weight
Periodo de tiempo: 0 and 6 months
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Change in weight in kgs between 0 and 6 months
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0 and 6 months
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TV Viewing Time
Periodo de tiempo: 0 and 6 months
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Change in self-reported TV viewing time per day between 0 and 6 months
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0 and 6 months
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Colaboradores e Investigadores
Aquí es donde encontrará personas y organizaciones involucradas en este estudio.
Patrocinador
Investigadores
- Investigador principal: Jeremy A Steeves, MS, University of Tennessee
- Silla de estudio: Dixie Lee Thompson, Phd, University of Tennessee
Publicaciones y enlaces útiles
La persona responsable de ingresar información sobre el estudio proporciona voluntariamente estas publicaciones. Estos pueden ser sobre cualquier cosa relacionada con el estudio.
Publicaciones Generales
- Steeves JA, Bassett DR, Fitzhugh EC, Raynor H, Cho C, Thompson DL. Physical Activity With and Without TV Viewing: Effects on Enjoyment of Physical Activity and TV, Exercise Self-Efficacy, and Barriers to Being Active in Overweight Adults. J Phys Act Health. 2016 Apr;13(4):385-91. doi: 10.1123/jpah.2015-0108. Epub 2015 Sep 17.
- Steeves JA, Bassett DR, Fitzhugh EC, Raynor HA, Thompson DL. Can sedentary behavior be made more active? A randomized pilot study of TV commercial stepping versus walking. Int J Behav Nutr Phys Act. 2012 Aug 6;9:95. doi: 10.1186/1479-5868-9-95.
Fechas de registro del estudio
Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.
Fechas importantes del estudio
Inicio del estudio
1 de septiembre de 2010
Finalización primaria (Actual)
1 de junio de 2011
Finalización del estudio (Actual)
1 de junio de 2011
Fechas de registro del estudio
Enviado por primera vez
21 de abril de 2011
Primero enviado que cumplió con los criterios de control de calidad
25 de abril de 2011
Publicado por primera vez (Estimar)
27 de abril de 2011
Actualizaciones de registros de estudio
Última actualización publicada (Estimar)
9 de noviembre de 2012
Última actualización enviada que cumplió con los criterios de control de calidad
10 de octubre de 2012
Última verificación
1 de octubre de 2012
Más información
Términos relacionados con este estudio
Palabras clave
Otros números de identificación del estudio
- UTennessee
Información sobre medicamentos y dispositivos, documentos del estudio
Estudia un producto farmacéutico regulado por la FDA de EE. UU.
No
Estudia un producto de dispositivo regulado por la FDA de EE. UU.
No
producto fabricado y exportado desde los EE. UU.
No
Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .